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International Journal of Bioprinting                                      3D-bioprinted meningioma model










































            Figure 5. In vivo tumorigenic characteristics of 3D-bioprinted meningioma microtissue in nude mice. (A) Growth condition of tumors in nude mice of
            both 3D-printed and 2D groups 40 days after inoculation with cells. (B) Observation of tumors removed from of a nude mouse of the 3D-printed group
            and another of the 2D group 40 days after inoculation with cells. (C, D) Comparison of tumor volumes between the 3D-printed and 2D groups at various
            time points (*p < 0.05, **p < 0.01, ***p < 0.005, ****p < 0.001).

            Furthermore, some genes expressed by tumor cells in 3D   cells and the ECM, between cells themselves, and between
            environments are related to signaling pathways associated   cells and signaling molecules.  These interactions have
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            with cell proliferation, migration, and transformation,   significant impacts on the growth and metastasis of tumor
            which are not expressed prominently in 2D environments.    cells. Our results demonstrate that IOMM-Lee cells grown
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            In our study, the mRNA and protein expression levels of   in 3D conditions are more invasive, with higher RNA and
            Ki67, p53, and EGFR were significantly higher in IOMM-  protein expression levels of N-cadherin, E-cadherin, and
            Lee cells under 3D conditions than in cells in the 2D group.   MMP9 than those of cells grown in 2D conditions. Previous
            Numerous studies have shown that the overexpression of   studies have also reported similar findings, showing that
            molecules such as Ki67, p53, and EGFR is closely related to   tumor cells grown in 3D conditions can secrete more
            the proliferation, invasion, and poor prognosis of malignant   secretory products,  such as  matrix metalloproteinases
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            meningiomas.  These findings  suggest that  tumor cells   and vascular  endothelial growth factor (VEGF) ; these
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            on  a 3D  bioprinting  platform may  better  maintain  their   molecules can degrade the ECM, promote angiogenesis,
            biological characteristics and gene expression profiles  in   and alter the structure of the ECM, thus promoting the
            vivo, which is important for understanding tumor biology   invasion and metastasis of tumor cells.  In summary,
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            and the development of tumor treatment.            tumor  cells  grown in  3D  culture  conditions  can better
               Considering the  closer resemblance  of the  gene   simulate the growth and metastatic process of tumors in
            expression profile of IOMM-Lee cells grown in a 3D   vivo and are thus more invasive.
            environment to that of  in vivo tumor cells, we further   In the investigation of tumor cell tumorigenicity, 3D
            investigated the biological characteristics of IOMM-  cultivation techniques have been widely used. Several
            Lee cells under 3D culture conditions. Compared to   studies have suggested that compared to 2D cultivation, 3D
            traditional 2D culture conditions, 3D culture conditions   cultivation better simulates the tumor microenvironment,
            better simulate the interactions between cells and their   enabling  a  more  precise  evaluation  of  tumor  cell
            surrounding environment, including interactions between   tumorigenicity. For instance, a study examining colon

            Volume 10 Issue 1 (2024)                       320                          https://doi.org/10.36922/ijb.1342
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